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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Plášť operační NADSTANDARD — 84 UDI-DI variants, MDR (CLINITEX s.r.o.)

MD Atlas
CLINITEX s.r.o.

Data from EUDAMED, last updated May 23, 2026

Plášť operační NADSTANDARD

859420696CLIX002SH

84 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: CLINITEX s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859420696CLIX002SH
Device name: Plášť operační NADSTANDARD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: CLINITEX s.r.o.
SRN: CZ-MF-000051598
Country: Czechia
Email: petr.bukovski@clinitex.cz
Phone: +420 602 721 937

Variants by status

UDI-DI variants

84 UDI-DI variants

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Applied filters

basicUdiUlid01KFNQ5N74T972VJPCDPH9JMGT

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

N16CAAA1KDUHAIB0010408594206966830
N16CAAA1KDUHAIB0000408594206966748
N16CAAA1KDUHAIB0090408594206966922
N16CAAA1KDUHAIB0010708594206966861
N16CAAA1KDUHAIB0000708594206966779
N16CAAA1KDUHAIB0090708594206966953
N16CAAA1KDUHAIB0010308594206966823
N16CAAA1KDUHAIB0000308594206966731
N16CAAA1KDUHAIB0090308594206966915

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